Healthonics, Inc. · Class II · Cleared Oct 10, 2003
| K-number | K030998 |
| Device name | MEDRELIEF SE SERIES, MODELS SE-50, SE-100, SE-200, SE-300 |
| Applicant | Healthonics, Inc. |
| Product code | IPF |
| Device class | Class II |
| Decision date | Oct 10, 2003 |
| Decision | Substantially Equivalent |
| Regulation | 890.5850 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov